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Articles in PresS, published online ahead of print November 21, 2001
Am J Physiol Gastrointest Liver Physiol, 10.1152/ajpgi.00291.2001
Submitted on July 13, 2001
Accepted on November 16, 2001
1 Physiology, The Chinese University of Hong Kong, Shatin, Hong Kong
2 Biochemistry, The Chinese University of Hong Kong, Shatin, Hong Kong
* To whom correspondence should be addressed. E-mail: whko{at}cuhk.edu.hk.
The effect of baicalein on mucosal ion transport in the rat distal colon was investigated in Ussing chambers. Mucosal addition of baicalein (1-100 µM) elicited a concentration-dependent ISC response. The increase in ISC was mainly due to Cl- secretion. The presence of mucosal indomethacin (10 µM) significantly reduced both the basal and subsequent baicalein-evoked ISC responses. The baicalein-induced ISC were inhibited by basolateral application of chromanol 293B (30µM), a blocker of KvLQT1 channels and Ba2+ ions (5mM). Treatment of the colonic mucosa with baicalein elicited a three-fold increase in cAMP production. Pretreating the colonic mucosa with carbachol (100 µM, serosal) but not thapsigargin (1 µM, both sides) abolished the baicalein-induced ISC. Addition of baicalein subsequent to forskolin induced a further increase in ISC. These results indicate that the baicalein-evoked Cl- secretion across rat colonic mucosa, possibly via cAMP-dependent pathway. However, the action of baicalein cannot be solely explained by its cAMP-elevating effect. Baicalein may stimulate Cl- secretion via a cAMP-independent pathway or have a direct effect on CFTR.
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